Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
01 2Centrient Pharmaceuticals Spain S.A.
02 1Apitoria Pharma Private Limited, Unit-IV
03 1Aurobindo Pharma Limited
04 2Lupin Ltd.
05 3North China Pharmaceutical Co., Ltd.
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
Registrant Name : Yuhan Corporation
Registration Date : 2015-07-03
Registration Number : 20140221-151-I-363-04(1)
Manufacturer Name : Centrient Pharmaceuticals Sp...
Manufacturer Address : Poligono Industrial Urvasa, C/Ripolles, 2 08130 Santa Perpetua de Mogoda (Barcelona),...
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2014-02-21
Registration Number : 20140221-151-I-363-04
Manufacturer Name : Centrient Pharmaceuticals Sp...
Manufacturer Address : C/Ripolles, n2 Poligono Industrial URVASA Santa Perpetua de Mogoda 08130 BARCELONA SP...
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PharmaCompass offers a list of Cephalexin Monohydrate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Cephalexin Monohydrate manufacturer or Cephalexin Monohydrate supplier for your needs.
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A Prindex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prindex, including repackagers and relabelers. The FDA regulates Prindex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prindex API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Prindex supplier is an individual or a company that provides Prindex active pharmaceutical ingredient (API) or Prindex finished formulations upon request. The Prindex suppliers may include Prindex API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Prindex Drug Master File in Korea (Prindex KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Prindex. The MFDS reviews the Prindex KDMF as part of the drug registration process and uses the information provided in the Prindex KDMF to evaluate the safety and efficacy of the drug.
After submitting a Prindex KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Prindex API can apply through the Korea Drug Master File (KDMF).
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